ComplianceOnline

Premarket Approval (PMA) agreement with FDA for the medical device companies - the Requirements

Instructor: E.J Smith
Product ID: 700955
  • Duration: 60 Min

recorded version

$249.00
1x Person - Unlimited viewing for 6 Months
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Recorded Link and Ref. material will be available in My CO Section
Last Recorded Date: Aug-2008

Training CD

$500.00
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(For multiple locations contact Customer Care)
CD and Ref. material will be shipped within 15 business days

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Read Frequently Asked Questions

This class reviews the modular option of filing a PMA and the benefits it offers all companies having to negotiate through the PMA process.

Most Class III devices require Premarket Approval (PMA) prior to marketing the device in the United States. This class reviews the modular option of filing a PMA and the benefits it offers all companies having to negotiate through the PMA process.

Areas Covered in the seminar:

  • Why a modular PMA.
  • Modular PMA agreement with the FDA.
  • Organizing each Module.
  • Review time for each module.
  • Manufacturing Module.
  • Clinical Module.
  • Class Audit of Manufacuring Facility up to 17 days.

Who will benefit:

This webinar is directed at all device, blood and biologist companies facing the PMA process and how best to dispense with each topic as the module is completed. Who will benefit:

  • Sponsor
  • Regulatory Manager
  • Clinical Specialist
  • Venture Capitalist

Instructor Profile

E.J. Smith, is a co-founder of Smith Associates, a FDA regulatory consulting firm that specializes in the preparation of 510(k), PMA and IDE submissions, device and cosmetic labeling, quality system audits and clinical trials. E.J. is the author of Hospital Consumables and Smith’s Reference and Illustrated Guide to Surgical Instruments and has 43 years of experience in medical marketing, executive positions and FDA regulatory affairs.

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Refund Policy

Registrants may cancel up to two working days prior to the course start date and will receive a letter of credit to be used towards a future course up to one year from date of issuance. ComplianceOnline would process/provide refund if the Live Webinar has been cancelled. The attendee could choose between the recorded version of the webinar or refund for any cancelled webinar. Refunds will not be given to participants who do not show up for the webinar. On-Demand Recordings can be requested in exchange.

Webinar may be cancelled due to lack of enrolment or unavoidable factors. Registrants will be notified 24hours in advance if a cancellation occurs. Substitutions can happen any time.

If you have any concern about the content of the webinar and not satisfied please contact us at below email or by call mentioning your feedback for resolution of the matter.

We respect feedback/opinions of our customers which enables us to improve our products and services. To contact us please email customercare@complianceonline.com call +1-888-717-2436 (Toll Free).

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